Assistant Ophthalmology Clinical Research Coordinator

Stanford University; Palo Alto (CA); Sur place; USD 37 000 - 69 000; Temps partiel

Avantages offerts par ce poste

PTO

Health benefits

Flexible work options

Tuition assistance

403(b) plan

Mental health programs

Commuter benefits

Résumé du poste

Stanford University’s Department of Ophthalmology is seeking an Assistant Clinical Research Coordinator to support clinical data collection and coordinate studies under PI supervision. The role is a 7-month fixed-term, 75% FTE (30 hours/week), with responsibilities across participant contact, data entry, regulatory documentation, and study logistics.

The successful candidate will assist with participant screening and consent, administer study instruments, collect specimens as required, and help

Qualifications

• Two-year college degree and one year of relevant experience or an equivalent combination of education and training.
• General knowledge of medical terminology.
• Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.

Responsabilités

• Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
• Prepare, distribute, and process questionnaires.
• Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.
• Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed.
• Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy.
• Extract data from source documents for research studies as directed. Collect data and complete case report forms.
• Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol.
• Prepare, process, and ship specimens/samples accurately under well-defined requirements.
• Order and maintain equipment and supplies.
• Process study compensation payments and thank you letters to subjects upon completion of trial activities. Assist with post-study activities, as needed.

Connaissances

Medical terminology

Data collection

Clerical skills

Formation

Two-year college degree + 1 year experience

Description du poste

Stanford University’s Department of Ophthalmology is seeking an Assistant Clinical Research Coordinator to support clinical data collection and coordinate studies under PI supervision. The role is a 7-month fixed-term, 75% FTE (30 hours/week), with responsibilities across participant contact, data entry, regulatory documentation, and study logistics.

The successful candidate will assist with participant screening and consent, administer study instruments, collect specimens as required, and help